Mono-N-glycosidation of β-Cyclodextrin − Synthesis of 6-(β-Cyclodextrinylamino)-6-deoxy-D-galactosides and of N-(6-Deoxy-β-cyclodextrinyl)galacto-azepane
✍ Scribed by Véronique Bonnet; Raphaël Duval; Vinh Tran; Claude Rabiller
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 216 KB
- Volume
- 2003
- Category
- Article
- ISSN
- 1434-193X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A modified beta-cyclodextrin bearing a 2-aminomethylpyridine binding site for copper(II) (6-deoxy-6-[N-(2-methylamino)pyridine)]-beta-cyclodextrin, CDampy) was synthesized by C6-monofunctionalization. The acid-base properties of the new ligand in aqueous solution were investigated by potentiometry a
## Abstract Protected morphine‐6‐glucuronide was converted into morphine‐[__N__‐methyl‐^14^C]‐6‐glucuronide by a three‐step procedure. Methyl (3‐pivaloylmorphin‐6‐yl 2,3,4‐tri‐__O__‐isobutyryl‐__β__‐D‐glucopyranosid)uronate was N‐demethylated by treatment with 1‐chloroethyl chloroformate to afford